4.0 - 7.0 years

0 Lacs

chennai, tamil nadu, india

On-site

JD Essential Experience & Qualifications A combination of experience that fulfills at least one of the following four criteria: 4-5 years of hands-on Detail Scheduling experience within the Pharmaceutical industry or Process Industry using SAP ECC or SAP APO. 4-5 years of Supply Planning experience in a Pharmaceutical industry or Process Industry using a hybrid of SAP APO and ECC. 6-7 years as a Business Analyst focusing on Production Planning & Execution in Pharmaceutical industry (Formulation or API). 6-7 years as an SAP PP and APO Functional Consultant within a Process or Pharmaceutical (Formulation) industry. Minimum of 1 year of hands-on, functional OMP OPR experience OR specifically wi...

Posted 2 days ago

AI Match Score

Apply

Master Data Technician II (2PM - 11 PM IST) Valvoline Global Operations

4.0 - 6.0 years

0 Lacs

gurugram, haryana, india

On-site

Job Purpose SAP Master Data Management, S4 HANA, MDG Tool How You Make An Impact (Job Accountabilities) Proficient in SAP ECC & S4 HANA. Proficient in MDG tool. Creation & Maintenance of Customer, Vendor and Material Master records. Perform mass updates on Customer, Vendor and Material Master data. Execute master data creation, updates and deletions in SAP Global master data domains. Creation & Maintenance of BOMs (Bill of Materials), Master recipes and Production versions. Creation and Maintenance of Pricing records using different Condition types and Condition tables in SAP Monitor, measure, and improve the quality of master data; identify data inconsistencies, duplicates, and inaccuracies...

Posted 2 days ago

AI Match Score

Apply

MQA upstream Associate Pfizer

2.0 - 5.0 years

0 Lacs

visakhapatnam, andhra pradesh, india

On-site

Key Responsibilities: Terminal Sterilization Block Operations (Solution/Emulsion Preparation, Vial/Ampoule Washing, Depyrogenation, Filling, Capping, and Collection) Ensure compliance with current Good Manufacturing Practices (cGMP) across all sterilization block operations Maintain regulatory standards and documentation in alignment with cGMP requirements Adhere to Pfizer manufacturing policies and procedures Review Electronic Batch Records (eBR) and assess AMPS (Agile Manufacturing Production System) exceptions with supervisor support Audit batch reports and equipment trails for accuracy and compliance Conduct alarm impact assessments and approve trend reports Monitor start-up and in-proce...

Posted 1 month ago

AI Match Score

Apply

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.